MX2019013010A - Maduracion de 1,4-bis(4-fenoxibenzoil)benceno. - Google Patents

Maduracion de 1,4-bis(4-fenoxibenzoil)benceno.

Info

Publication number
MX2019013010A
MX2019013010A MX2019013010A MX2019013010A MX2019013010A MX 2019013010 A MX2019013010 A MX 2019013010A MX 2019013010 A MX2019013010 A MX 2019013010A MX 2019013010 A MX2019013010 A MX 2019013010A MX 2019013010 A MX2019013010 A MX 2019013010A
Authority
MX
Mexico
Prior art keywords
bis
phenoxybenzoylbenzene
phase
lewis acid
phenoxybenzoyl
Prior art date
Application number
MX2019013010A
Other languages
English (en)
Inventor
Jouanneau Julien
Amstutz Jérome
Vincent Guillaume
Original Assignee
Arkema France
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Arkema France filed Critical Arkema France
Publication of MX2019013010A publication Critical patent/MX2019013010A/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/45—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation
    • C07C45/46—Friedel-Crafts reactions
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
    • C07C45/30—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with halogen containing compounds, e.g. hypohalogenation
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/41—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by hydrogenolysis or reduction of carboxylic groups or functional derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/51—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/78—Separation; Purification; Stabilisation; Use of additives
    • C07C45/79—Separation; Purification; Stabilisation; Use of additives by solid-liquid treatment; by chemisorption
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/78—Separation; Purification; Stabilisation; Use of additives
    • C07C45/81—Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
    • C08G61/127—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from carbon dioxide, carbonyl halide, carboxylic acids or their derivatives
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
    • C08G65/38—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols
    • C08G65/40—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols from phenols (I) and other compounds (II), e.g. OH-Ar-OH + X-Ar-X, where X is halogen atom, i.e. leaving group
    • C08G65/4012—Other compound (II) containing a ketone group, e.g. X-Ar-C(=O)-Ar-X for polyetherketones
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
    • C08G65/38—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols
    • C08G65/40—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols from phenols (I) and other compounds (II), e.g. OH-Ar-OH + X-Ar-X, where X is halogen atom, i.e. leaving group
    • C08G65/4012—Other compound (II) containing a ketone group, e.g. X-Ar-C(=O)-Ar-X for polyetherketones
    • C08G65/4043—(I) or (II) containing oxygen other than as phenol or carbonyl group
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L65/00—Compositions of macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain; Compositions of derivatives of such polymers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
    • C08G2261/34—Monomer units or repeat units incorporating structural elements in the main chain incorporating partially-aromatic structural elements in the main chain
    • C08G2261/344—Monomer units or repeat units incorporating structural elements in the main chain incorporating partially-aromatic structural elements in the main chain containing heteroatoms
    • C08G2261/3442—Polyetherketones
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/40—Polymerisation processes
    • C08G2261/45—Friedel-Crafts-type

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Polyethers (AREA)

Abstract

La invención se refiere a un método para fabricar 1,4-bis (4-fenoxibenzoil)benceno, que comprende: hacer reaccionar cloruro de tereftaloilo con difenil éter en un solvente de reacción y en la presencia de un ácido de Lewis, para obtener una mezcla de producto que comprende un Complejo de 1,4-bis(4-fenoxibenzoil)benc eno-ácido de Lewis; poner en contacto la mezcla del producto con un solvente prótico, para obtener una primera fase que contiene el ácido de Lewis y una segunda fase que contiene 1,4-bis(4-fenoxibenzoil)benceno; calentar por lo menos la segunda fase hasta una temperatura máxima, seguido de enfriar la segunda fase hasta una temperatura de separación; sometiendo por lo menos la segunda fase a un paso de separación sólido/líquido a la temperatura de separación, para recuperar 1,4-bis(4-fenoxibenzoil) benceno sólido.
MX2019013010A 2017-05-18 2018-05-17 Maduracion de 1,4-bis(4-fenoxibenzoil)benceno. MX2019013010A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP17305582.3A EP3404012B1 (en) 2017-05-18 2017-05-18 Ripening of 1,4-bis (4-phenoxybenzoyl)benzene
PCT/EP2018/063017 WO2018211048A1 (en) 2017-05-18 2018-05-17 Ripening of 1,4-bis (4-phenoxybenzoyl) benzene

Publications (1)

Publication Number Publication Date
MX2019013010A true MX2019013010A (es) 2020-02-05

Family

ID=58779048

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2019013010A MX2019013010A (es) 2017-05-18 2018-05-17 Maduracion de 1,4-bis(4-fenoxibenzoil)benceno.

Country Status (10)

Country Link
US (2) US10981852B2 (es)
EP (2) EP3404012B1 (es)
JP (1) JP2020520362A (es)
KR (1) KR102416475B1 (es)
CN (1) CN110637004B (es)
BR (1) BR112019022946A2 (es)
CA (1) CA3061562A1 (es)
MX (1) MX2019013010A (es)
RU (1) RU2019141826A (es)
WO (1) WO2018211048A1 (es)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2829265T3 (es) 2017-05-16 2021-05-31 Arkema France Método para fabricar 1,4-bis(4-fenoxibenzoil)benceno a una temperatura elevada
ES2829260T3 (es) 2017-05-16 2021-05-31 Arkema France Método para fabricar 1,4-bis(4-fenoxibenzoil)benceno usando cloruro de tereftaloílo sustancialmente no hidrolizado
EP3404011B1 (en) 2017-05-18 2020-08-26 Arkema France Dissociation of a 1,4-bis(4-phenoxybenzoyl)benzene-lewis acid-complex in an aqueous solution
US10793500B2 (en) * 2017-05-16 2020-10-06 Arkema France Dissociation of 1,4-bis (4-phenoxybenzoyl)benzene—Lewis acid complex in a protic solvent
EP3650433B1 (en) 2018-11-09 2024-04-24 Arkema France Method for manufacturing 1,4-bis (4-phenoxybenzoylbenzene) at an elevated temperature

Family Cites Families (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SU445643A1 (ru) 1973-01-08 1974-10-05 Институт Высокомолекулярных Соединений Ан Ссср Способ получени 1,4-бис(4-феноксибензоил)бензола
SU626555A1 (ru) 1973-03-05 1979-07-25 Институт высокомолекулярных соединений 1,4 Бис (4-ацетил-4-феноксибензоил) бензол-мономер дл прочного при изгибе и термостойкого полимера
SU638588A1 (ru) 1977-06-28 1978-12-25 Ярославский политехнический институт Способ получени 1,4-бис(4 -феноксибензоил)-бензола
US4709007A (en) 1983-03-31 1987-11-24 Raychem Corporation Preparation of aromatic polymers
US4816556A (en) 1985-02-22 1989-03-28 E. I. Du Pont De Nemours And Company Ordered polyetherketones
CA1246297A (en) 1985-03-11 1988-12-06 Robert A. Clendinning Process for preparing poly(aryl ether ketones)
US4716211A (en) 1985-03-11 1987-12-29 Amoco Corporation Slurry process for producing high molecular weight crystalline polyaryletherketones
US4891167A (en) 1985-05-02 1990-01-02 Amoco Corporation Block polymers containing a poly(aryl ether ketone) and methods for their production
US4704448A (en) 1985-11-25 1987-11-03 E. I. Du Pont De Nemours And Company Copolyetherketones
US5137988A (en) 1986-07-25 1992-08-11 Amoco Corporation Amino-terminated poly(aryl ether ketones)
DE3789354T2 (de) 1986-11-20 1994-08-04 Asahi Chemical Ind Aromatischer Polyether und Verfahren zur Herstellung eines Polyethers.
JPS63258923A (ja) 1987-04-16 1988-10-26 Asahi Chem Ind Co Ltd 芳香族ポリエ−テルケトンの製造方法
US4826947A (en) 1987-07-09 1989-05-02 Raychem Corporation Preparation of poly(arylene ether ketones)
US4794155A (en) * 1987-08-26 1988-12-27 The Dow Chemical Company Process for forming arylether polymers
US4835319A (en) 1987-11-09 1989-05-30 E. I. Du Pont De Nemours And Company Process for the manufacture of 1,4-bis(4-phenoxybenzoyl)benzene with a zeolite catalyst
US4827041A (en) 1988-03-10 1989-05-02 E. I. Du Pont De Nemours And Company Process for the manufacture of 1,4-bis(4-phenoxybenzoyl)benzene with a perfluorosulfonyl resin catalyst
US4918237A (en) * 1989-03-13 1990-04-17 E. I. Du Pont De Nemours And Company Process for the manufacture of 1,4-bis(4-phenoxybenzoyl)benzene with certain metal-containing catalysts
US5258491A (en) 1992-09-04 1993-11-02 Eastman Kodak Company Process for preparation of a polyetherketone
GB9403944D0 (en) 1994-03-02 1994-04-20 Victrex Manufacturing Ltd Aromatic polymers
FR2993567B1 (fr) 2012-07-20 2015-09-25 Arkema France Procede de synthese de poly-aryl-ether-cetones
EP3404011B1 (en) 2017-05-18 2020-08-26 Arkema France Dissociation of a 1,4-bis(4-phenoxybenzoyl)benzene-lewis acid-complex in an aqueous solution
ES2774725T3 (es) 2017-05-16 2020-07-22 Arkema France Método de fabricación de 1,4-bis(4-fenoxibenzoil)benceno en condiciones de sobresaturación
EP3404013B1 (en) 2017-05-18 2021-10-27 Arkema France Purification of 1,4-bis (4-phenoxybenzoyl)benzene by centrifugal filtration
ES2829260T3 (es) 2017-05-16 2021-05-31 Arkema France Método para fabricar 1,4-bis(4-fenoxibenzoil)benceno usando cloruro de tereftaloílo sustancialmente no hidrolizado
ES2829265T3 (es) 2017-05-16 2021-05-31 Arkema France Método para fabricar 1,4-bis(4-fenoxibenzoil)benceno a una temperatura elevada
US10793500B2 (en) 2017-05-16 2020-10-06 Arkema France Dissociation of 1,4-bis (4-phenoxybenzoyl)benzene—Lewis acid complex in a protic solvent
EP3438085A1 (en) 2017-08-04 2019-02-06 Arkema France Process for producing polyether ketone ketone

Also Published As

Publication number Publication date
JP2020520362A (ja) 2020-07-09
BR112019022946A2 (pt) 2020-06-09
EP3404012A1 (en) 2018-11-21
WO2018211048A1 (en) 2018-11-22
US20190152886A1 (en) 2019-05-23
CA3061562A1 (en) 2018-11-22
CN110637004A (zh) 2019-12-31
KR20200009037A (ko) 2020-01-29
EP3625207A1 (en) 2020-03-25
CN110637004B (zh) 2023-04-18
EP3404012B1 (en) 2020-09-09
US10981852B2 (en) 2021-04-20
RU2019141826A (ru) 2021-06-18
KR102416475B1 (ko) 2022-07-01
US20210155570A1 (en) 2021-05-27

Similar Documents

Publication Publication Date Title
MX2019013010A (es) Maduracion de 1,4-bis(4-fenoxibenzoil)benceno.
MX2019013011A (es) Purificacion de 1,4-bis(4-fenoxibenzoil)benceno mediante filtracion por centrifugacion.
MX2019012998A (es) Metodo para manufacturar 1,4-bis(4-fenoxibenzoil)benceno a una temperatura elevada.
MX2019012999A (es) Metodo para fabricar 1,4-bis(4-fenoxibenzoil)benceno en condiciones de supersaturacion.
MX2019013003A (es) Disociacion de un complejo de 1,4-bis(4-fenoxibenzoil)benceno-acid o de lewis en una solucion acuosa.
AU2014366334B2 (en) Mono- and dialkyl ethers of furan-2,5-dimethanol and (tetra-hydrofuran-2,5-diyl)dimethanol and amphiphilic derivatives thereof
MX2019013005A (es) Metodo para fabricar el 1,4-bis(4-fenoxibenzoil)benceno con el uso de cloruro de tereftaloilo sustancialmente no hidrolizado.
MX2012012496A (es) Metodo para producir tetrafluoropropenos.
MX2013013144A (es) Metodo para la produccion de un dimero mdi.
AR093155A1 (es) Metodos para la produccion de 5-(halometil)furfural
MX2015013012A (es) Isomerizacion a alta temperatura de (e)-1-cloro-3,3,3-trifluroprop eno a (z)-1-cloro-3,3,3-trifluoropropeno.
MX2018002031A (es) Proceso para la preparacion de 1,4-bis (etoximetil) ciclohexano.
MY169158A (en) Method for manufacturing succinic acid estres
WO2018002798A3 (en) Process for the preparation of dialkyl terephthalates from recycle feedstocks
KR101627039B1 (ko) 로듐 촉매를 이용한 퓨로피란온 유도체의 원-팟 합성방법
MX2017011790A (es) Metodo para fabricar acido furan-2,5-dicarboxilico (fdca) a partir de una sal solida.
CN105646140A (zh) 一种1,2,4,5-四氟苯的制备方法
CN104558517A (zh) 双酚a型环氧树脂合成方法
WO2017180240A8 (en) Production of methyl-substituted biphenyl compounds
CN106117127A (zh) 医药原料1,4-二溴吡啶的合成方法
MY186195A (en) Process for producing crude palm fruit oil
CN106518692A (zh) 医用中间体3‑氨基‑4‑溴苯酚的合成方法
TH165097A (th) วิธีการสำหรับการกำจัดปรอทออกจากวัตถุดิบป้อนซึ่งประกอบด้วยไฮโดรคาร์บอน ชนิดหนักซึ่งอยู่ส่วนต้นของ หน่วยกลั่นลำดับส่วน
CN106117029A (zh) 医药原料3-氢氯酸-2-氟苯乙醛的合成方法
Demaison 382 C 4 Cl 2 F 4 1, 2-Dichloro-3, 3, 4, 4-tetrafluorocyclobutene: Molecular Constants